QC Analyst


Title:  QC Analyst
Location:  East Windsor, NJ
Duration:  Contract
Schedule:  M-F 3rd shift need 9:30PM-6:30AM
Target Start Date:  ASAP

Must haves:  
  • High School diploma with 5 to 8 years’ experience in a QC laboratory under GMP or bachelor’s degree in chemistry or related science degree with no minimum QC laboratory under GMP experience required. 
  • Working knowledge of analytical theory and techniques and familiarity with GMP procedures required for the laboratory work. 
  • Capable of analysis and reasoning. 
  • Sense of ownership and pride in work. 
  • Critical, detailed and organized. 
  • Self-motivated, collaborative and team player

Responsibilities:
  • Ensures all Quality Control (QC) activities at the technical transfer center (TTC) are carried out in compliance with Corporate Operating Procedures (COP Standard operating procedures (SOP), Internal Operating Procedures (IOP), and Federal Food and Drug Administration (FDA), International Conference on Harmonization (ICH), Occupational Safety and Health Administration (OSHA), and Environmental Protection Agency (EPA) requirements.
  • Responsible for contributing to the success of each project by meeting the requirements of the project team and supplying the necessary analytical chemistry know how in routine quality control analysis, technical transfer and/or validation of the analytical methods. 
  • Provide the analytical results and adequate pro-active interpretation to help enrich the team’s understanding of the project.
  • Follow the assignments from the Team Leader, on time and with quality. 
  • Perform analytical testing (i.e. raw materials, intermediates, API, stability, cleaning, method validation and cleaning) in a timely manner to meet deadlines. 
  • Execute qualification test contained in protocols for equipment qualification. 
  • Perform instrument calibrations on Balances, High Pressure Liquid Chromatography (HPLC), and Gas Chromatography (GC). 
  • Maintains equipment, project, and general QC logbooks. 
  • Proposes changes for continuous improvement, either in safety, GMPs, or general QC efficiency. 
  • Communicate with management concerning all HSE issues. 
  • Participate in monthly GMP audits and weekly safety audits as delegated by QC Management. 
 

Joule, a System One division is a leader in specialized workforce solutions and integrated services. With more than 6,000 employees and roughly 50 offices throughout the U.S. we provide scientific, clinical, engineering, energy, IT, legal and administrative staffing services. For more than 40 years, we have delivered workforce solutions and integrated services to clients nationally.


Company
System One
Posted
10/06/2021
Type
Full time
Salary Range
$43,000.00 - 63,000.00
per Year
Salary range estimated by
Location
Hightstown, NJ 08520, US
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